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FIGURE 3 in The arboreal tiger beetles (Coleoptera: Cicindelidae) of Sri Lanka recorded from recent investigations
FIGURE 3. Tricondyla (Indotricondyla) granulifera Female Dorsal view
FIGURE 2 in The arboreal tiger beetles (Coleoptera: Cicindelidae) of Sri Lanka recorded from recent investigations
FIGURE 2. Tricondyla (Indotricondyla) gounellei Male
FIGURE 8 in The arboreal tiger beetles (Coleoptera: Cicindelidae) of Sri Lanka recorded from recent investigations
FIGURE 8. Derocrania (Derocrania) schaumi Female
FIGURE 4 in The arboreal tiger beetles (Coleoptera: Cicindelidae) of Sri Lanka recorded from recent investigations
FIGURE 4. Tricondyla (Indotricondyla) granulifera Female Lateral view
FIGURE 11 in The arboreal tiger beetles (Coleoptera: Cicindelidae) of Sri Lanka recorded from recent investigations
FIGURE 11. Neocollyris (Stenocollyris) vedda Male
FIGURE 12 in The arboreal tiger beetles (Coleoptera: Cicindelidae) of Sri Lanka recorded from recent investigations
FIGURE 12. Neocollyris (Stenocollyris) vedda Male Lateral view
FIGURE 13 in The arboreal tiger beetles (Coleoptera: Cicindelidae) of Sri Lanka recorded from recent investigations
FIGURE 13. Neocollyris (Stenocollyris) vedda Male Head region
FIGURE 5 in The arboreal tiger beetles (Coleoptera: Cicindelidae) of Sri Lanka recorded from recent investigations
FIGURE 5. Tricondyla (Indotricondyla) femorata Male
FIGURE 6 in The arboreal tiger beetles (Coleoptera: Cicindelidae) of Sri Lanka recorded from recent investigations
FIGURE 6. Derocrania (Derocrania) concinna Female
FIGURE 7 in The arboreal tiger beetles (Coleoptera: Cicindelidae) of Sri Lanka recorded from recent investigations
FIGURE 7. Derocrania (Derocrania) halyi Male
Figure 1 in Potomida littoralis (Bivalvia, Unionidae) evolutionary history: slow evolution or recent speciation?
Figure 1. Distribution of Potomida littoralis. Numbered points show sampling localities.
Weather dataset (Typical Downscaled Year, Extreme Cold Year, Extreme Warm Year) for building energy simulations (.epw format) in recent past climate, Sint-Katelijne-Waver, Belgium
<p>Typical Downscaled Year (TDY), Extreme Cold Year and Extreme Warm Year based on the methodology of Nik (2016), is extracted for the location of Sint-Katelijne-Waver (51°3'25"N 4°11'24" E) from the EC-Earth driven convection-permitting climate model COSMO-CLM for the Belgian domain extended with land-surface scheme TERRA_URB(v2.0) making use of the SURY (Semi-empirical URban canopY) parameterization ( Wouters et al. 2016). The integrations are identical to the ones which are described in Vanden Broucke et al. (2019). The climate model has a spatial resolution of 2.8 km and an hourly temporal resolution and is available for the recent past (1976-2004) and future (2070-2098) as 30-year datasets. For this dataset, the TDY, ECY, and EWY are extracted for the recent past period. A bias correction is applied for the following variables: temperature (as described in Ramon et al. 2020), solar radiation and relative humidity as described in Ramon et al. (202X).</p>
Predator presence and recent climatic warming raise body temperatures of island lizards
<p>In ectothermic predator-prey relationships, evasion of predation by prey depends on physiological and behavioural responses relating to the thermal biology of both predator and prey. On Japan's Izu Islands, we investigated a prey lizard's physiological and thermal responses to the presence of a snake predator over geologic time in addition to recent climatic warming. Foraging lizard body temperatures increased by 1.0°C from 1981 to 2019 overall, yet were 2.9°C warmer on snake islands relative to snake-free islands. We also detected snake predator-induced selection on hind leg length, which in turn is a major determinant for sprint speed only in lizard populations exposed to predation by snakes. Accordingly, we found that warmer prey body temperatures result in faster sprint speeds by the prey at temperatures suboptimal for the snake predator, and therefore contribute to escaping predation. Given recent climatic change, further warming could irrevocably alter this and other ectothermic predator-prey relationships.</p>
Recent Advances and Perspectives in Photodriven Charge Accumulation in Molecular Compounds: A Mini Review
<p>Source files for figures in the publication in <em>Energy Fuels</em><em> </em><strong>2021</strong>, <em>35</em>, 18848–18856.</p> <p>https://pubs.acs.org/doi/10.1021/acs.energyfuels.1c02073</p>
FIGURE 15A–C in Illustrations and taxonomic placement of the Recent Fusus and Fasciolaria in the Lamarck collection of the Muséum d'Histoire Naturelle, Geneva
FIGURE 15A–C. Three possible syntypes of Fusus buccinatus, MHNG INVE 51737.
FIGURE 20A–B. Fusus scalarinus, MHNG INVE 51739 in Illustrations and taxonomic placement of the Recent Fusus and Fasciolaria in the Lamarck collection of the Muséum d'Histoire Naturelle, Geneva
FIGURE 20A–B. Fusus scalarinus, MHNG INVE 51739.
FIGURE 18A–C. Fusus lignarius, MHNG INVE 51729 in Illustrations and taxonomic placement of the Recent Fusus and Fasciolaria in the Lamarck collection of the Muséum d'Histoire Naturelle, Geneva
FIGURE 18A–C. Fusus lignarius, MHNG INVE 51729.
FIGURE 16A–B.Fusus coronatus. minor, MHNG INVE 51723 in Illustrations and taxonomic placement of the Recent Fusus and Fasciolaria in the Lamarck collection of the Muséum d'Histoire Naturelle, Geneva
FIGURE 16A–B.Fusus coronatus. minor, MHNG INVE 51723.
FIGURE 14A–C in Illustrations and taxonomic placement of the Recent Fusus and Fasciolaria in the Lamarck collection of the Muséum d'Histoire Naturelle, Geneva
FIGURE 14A–C. Three possible syntypes of Fusus buccinatus, MHNG INVE 51737.
FIGURE 13A–C. Fusus articulatus, MHNG INVE 51736 in Illustrations and taxonomic placement of the Recent Fusus and Fasciolaria in the Lamarck collection of the Muséum d'Histoire Naturelle, Geneva
FIGURE 13A–C. Fusus articulatus, MHNG INVE 51736.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.